Canonical Allele Identifier: CA1950237085

Gene: TPP1

Linked Data

• dbSNP Id: rs1855590060

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.6616657del , CM000673.2:g.6616657del	GRCh38
NC_000011.9:g.6637888del , CM000673.1:g.6637888del	GRCh37
NC_000011.8:g.6594464del	NCBI36
NG_008653.1:g.7805del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682424.1:c.772+4del	ENSP00000507321.1:n.772+4del
ENST00000299427.12:c.886+4del MANE Select	ENSP00000299427.6:n.886+4del
ENST00000436873.7:c.313-583del
ENST00000524788.2:n.2049del
ENST00000524903.2:n.2165del
ENST00000528807.2:n.546del
ENST00000530040.2:n.480-154del
ENST00000533371.6:c.157+4del	ENSP00000437066.1:n.157+4del
ENST00000642892.1:c.157+4del	ENSP00000494165.1:n.157+4del
ENST00000643439.1:c.*626+4del	ENSP00000495849.1:n.*626+4del
ENST00000643479.1:n.919del
ENST00000643516.1:c.396-154del
ENST00000644151.1:n.2329del
ENST00000644218.1:c.886+4del	ENSP00000493574.1:n.886+4del
ENST00000644683.1:c.*339+4del	ENSP00000494085.1:n.*339+4del
ENST00000644810.1:c.607+4del	ENSP00000495895.1:n.607+4del
ENST00000644831.1:n.1062+4del
ENST00000644933.1:c.157+4del	ENSP00000496133.1:n.157+4del
ENST00000645020.1:n.2180del
ENST00000645285.1:c.157+4del	ENSP00000495058.1:n.157+4del
ENST00000645331.1:n.1256del
ENST00000645620.1:c.157+4del	ENSP00000493657.1:n.157+4del
ENST00000646777.1:n.1066del
ENST00000647016.1:n.1366+4del
ENST00000647152.1:c.157+4del	ENSP00000495893.1:n.157+4del
ENST00000647209.1:c.*755+4del	ENSP00000495558.1:n.*755+4del
ENST00000647346.1:n.1906+4del
ENST00000299427.10:c.886+4del	ENSP00000299427.6:n.886+4del
ENST00000436873.6:c.451-154del	ENSP00000398136.2:n.451-154del
ENST00000528807.1:n.440del
ENST00000533371.5:c.157+4del	ENSP00000437066.1:n.157+4del
ENST00000611494.4:c.886+4del	ENSP00000484546.1:n.886+4del
NM_000391.3:c.886+4del	NP_000382.3:n.886+4del
NM_000391.4:c.886+4del MANE Select	NP_000382.3:n.886+4del